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SWI/SNF亚基突变导致肿瘤发生机制中的新出现主题

Emerging Themes in Mechanisms of Tumorigenesis by SWI/SNF Subunit Mutation.

作者信息

Jones Cheyenne A, Tansey William P, Weissmiller April M

机构信息

Department of Biology, Middle Tennessee State University, Murfreesboro, TN, USA.

Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN, USA.

出版信息

Epigenet Insights. 2022 Jul 26;15:25168657221115656. doi: 10.1177/25168657221115656. eCollection 2022.

Abstract

The SWI/SNF chromatin remodeling complex uses the energy of ATP hydrolysis to alter contacts between DNA and nucleosomes, allowing regions of the genome to become accessible for biological processes such as transcription. The SWI/SNF chromatin remodeler is also one of the most frequently altered protein complexes in cancer, with upwards of 20% of all cancers carrying mutations in a SWI/SNF subunit. Intense studies over the last decade have probed the molecular events associated with SWI/SNF dysfunction in cancer and common themes are beginning to emerge in how tumor-associated SWI/SNF mutations promote malignancy. In this review, we summarize current understanding of SWI/SNF complexes, their alterations in cancer, and what is known about the impact of these mutations on tumor-relevant transcriptional events. We discuss how enhancer dysregulation is a common theme in SWI/SNF mutant cancers and describe how resultant alterations in enhancer and super-enhancer activity conspire to block development and differentiation while promoting stemness and self-renewal. We also identify a second emerging theme in which SWI/SNF perturbations intersect with potent oncoprotein transcription factors AP-1 and MYC to drive malignant transcriptional programs.

摘要

SWI/SNF染色质重塑复合体利用ATP水解产生的能量来改变DNA与核小体之间的相互作用,使基因组区域能够参与转录等生物学过程。SWI/SNF染色质重塑因子也是癌症中最常发生改变的蛋白质复合体之一,超过20%的癌症在SWI/SNF亚基中携带突变。在过去十年中,深入的研究探索了与癌症中SWI/SNF功能障碍相关的分子事件,肿瘤相关的SWI/SNF突变如何促进恶性肿瘤的常见模式也开始显现。在这篇综述中,我们总结了目前对SWI/SNF复合体的认识、它们在癌症中的改变,以及这些突变对肿瘤相关转录事件影响的已知情况。我们讨论了增强子失调如何成为SWI/SNF突变型癌症的一个共同特征,并描述了增强子和超级增强子活性的相应改变如何共同阻碍发育和分化,同时促进干性和自我更新。我们还确定了第二个新出现的主题,即SWI/SNF扰动与强大的癌蛋白转录因子AP-1和MYC相互作用,以驱动恶性转录程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78f9/9329810/881fd173da58/10.1177_25168657221115656-fig1.jpg

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